What I Wish Everyone Knew About C6H17NO3Si

The prevalence of solvent effects in heterogeneous catalysis in condensed media has motivated developing quantitative kinetic, their interactions with reaction intermediates and transition states. I hope my blog about 13822-56-5 is helpful to your research. Name: 3-(Trimethoxysilyl)propan-1-amine.

Chemistry graduates have much scope to use their knowledge in a range of research sectors, including roles within chemical engineering, chemical and related industries, healthcare and more. 13822-56-5, Name is 3-(Trimethoxysilyl)propan-1-amine, molecular formula is C6H17NO3Si, Name: 3-(Trimethoxysilyl)propan-1-amine, SMILES is NCCC[Si](OC)(OC)OC belongs to naphthyridine compound, is a common compound. In a patnet, author is Shaabani, Ahmad, once mentioned the new application about 13822-56-5.

The diversity-oriented synthesis of a naphthyridine scaffold has been demonstrated via a novel domino four-component reaction. The syntheses were achieved by reacting a diamine, 1,1-bis(methylthio)-2-nitroethylene, 2-aminoprop-1-ene-1,1,3-tricarbonitrile, and various carbonyl compounds using a deep eutectic solvent (DES), based on choline chloride/urea, thus providing a new class of poly-functionalized fused naphthyridine derivatives with the concomitant formation of three new rings and six sigma bonds. The reaction conditions were mild and did not require additional base catalysts. Given the inexpensive, nontoxic, and recyclable nature of the DES, these reaction conditions are simple and highly environmentally friendly. (C) 2015 Elsevier Ltd. All rights reserved.

The prevalence of solvent effects in heterogeneous catalysis in condensed media has motivated developing quantitative kinetic, their interactions with reaction intermediates and transition states. I hope my blog about 13822-56-5 is helpful to your research. Name: 3-(Trimethoxysilyl)propan-1-amine.

Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem